A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv269n111



Internal ID22798469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:129096756..129124380hg38UCSC Ensembl
chr8:130109002..130136626hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3827625
hg1927625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1161799, nsv1161800
Samples
Known Genes
MethodSNP array
Analysis1) We applied common software Birdsuite to detect genome-wide CNVs; 2) we used our algorithm WinXPCNVer which is based on probe intensity to identify Tibetan specific CNV; 3) we further genotyped the discovered Tibetan specific CNV by K-means and manual observation.
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceLou_et_al_2015
Pubmed ID26073780
Accession Number(s)dgv269n111
Frequency
Sample Size369
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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